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Comparison of three methods for detection of Plasmodium oocysts in wild-caught mosquitoes

Published online by Cambridge University Press:  19 September 2011

D. Edoh
Affiliation:
Swiss Tropical Institute, Socinstrasse 57, Postfach, 4002 Basel, Switzerland
H. Haji
Affiliation:
Ifakara Centre, Box 53, Ifakara, Tanzania
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Abstract

One hundred forty-nine Anopheles gambicie s.l. and 260 A. funestus were collected from the field in Namawala, Tanzania in June 1994. The mosquitoes were dissected and examined for plasmodium oocysts using two microscopic techniques and the polymerase chain reaction (PCR) method. The oldest and simplest technique, the saline test, detected oocysts in 94 out of the 97 mosquitoes found to have oocysts by the more sensitive merbromin stain and PCR techniques. The saline test was found to be a sensitive and reliable field technique for detection of large Plasmodium oocysts in mosquitoes. The merbromin staining technique was as sensitive as PCR, detecting even small oocysts.

Résumé

Cent quarante-neuf Anopheles gambiae s.l. et deux cent soixante (260) A. funestus ont été collectées en juin 1994, dans un champ à Namawala en Tanzanie. Les moustiques étaient disséqués et examinés pour la détection des oocysts de Plasmodium par deux techniques microscopiques et par la méthode de réaction de la chaîne polymérase (RCP). L'emploi de la solution saline, une technique très ancienne et très simple, a permis de détecter des oocytes chez 94 des 97 moustiques ayant déjà témoigne de la présence des oocysts par les techniques très sensibles: les traces de merbromine et la RCP. Le test par la solution saline s'est révélé être une technique sensible et faible de terrain pour détecter de gros oocytes chez les moustiques infectés de Plasmodium. La technique des traces de merbromine était aussi sensible que la RCP détectant même les petits oocytes.

Type
Research Articles
Copyright
Copyright © ICIPE 1998

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References

Babiker, H. A., Ranford-Cartwright, L. C., Currie, D., Charlwood, J. D., Billingsley, P., Teuscher, T. and Walliker, D. (1994) Random mating in a natural population of the malaria parasite Plasmodium falcipamm. Parasitol. 109, 413421.CrossRefGoogle Scholar
Baker, R. H. Jr (1993) Use of PCR in the field. Parasitol. Today 10, 117119.CrossRefGoogle Scholar
Baker, R. H., Banchongaksorn, T., Courval, J. M., Suwonkerd, W., Rimwungtragoon, K., Srittong, N. and Wirth, D. F. (1994) DNA probes as epidemiologie tools for surveillance of Plasmodium falcipamm malaria in Thailand. Int. J. Epidemiol. 23, 161168.CrossRefGoogle Scholar
Beier, J. C., Oster, C. N., Onyango, F. K., Bales, J. D., Sherwood, J. A., Perkins, P. V., Chumo, D. K., Koech, D. V., Whitmire, R. E., Roberts, C. R. and Diggs, C. R. (1994) Plasmodium falciparum incidence relative to entomological inoculation rates at a site proposed for testing malaria vaccines in western Kenya. Am. J. Trop. Med. Hyg. 50, 529536.CrossRefGoogle Scholar
Burkot, T. R., Zavala, F., Gwadz, R. W., Collins, F. W., Nussenzweig, R. S. and Roberts, D. R. (1984) Identification of malaria infected mosquitoes by a two-site enzyme-linked immunosorbent assay. Am. J. Trop. Med. Hyg. 33, 227231.CrossRefGoogle ScholarPubMed
Edoh, D. (1995) Rejoinder: The use of PCR in the field. Parasitol. Today 11, 68.CrossRefGoogle ScholarPubMed
Githeko, A. K., Brandling-Bennett, A. D., Beier, M., Atieli, F., Owaga, M. and Collins, F. W. (1992) The reservoir of Plasmodium falcipamm in a holoendemic area of western Kenya. Trans. R. Soc. Trop. Med. Hyg. 86, 355358.CrossRefGoogle Scholar
Kain, K. C. and Lanar, D. E. (1991) Determination of genetic variation within Plasmodium falcipamm by using enzymatically amplified DNA from filter paper disks impregnated with whole blood, J. Clin. Microbiol. 26, 11711174.CrossRefGoogle Scholar
Ranford-Cartwright, L. C., Balfe, P., Carter, R. and Walliker, D. (1991) Genetic hybrids of Plasmodium identified by amplification of genomie DNA from single oocysts. Mol. Biochem. Parasitol. 49, 239244.CrossRefGoogle Scholar
Ranford-Cartwright, L. C., Balfe, P., Carter, R. and Walliker, D. (1993) Frequency of cross-fertilization in thehuman malaria parasite Plasmodium falcipamm. Parasitol. 107, 1118.CrossRefGoogle Scholar
Rodgers, M. R., Popper, S. J. and Wirth, D. F. (1990) Amplification of kinetoplast DNA as a tool in the detection and diagnosis of Leishmania. Exp. Parasitol. 71, 267275.CrossRefGoogle ScholarPubMed
Smith, T., Charlwood, J. D., Kihonda, J., Mwankuyse, S., Billingsley, P., Meuwissen, J., Lyimo, E., Takken, W., Teuscher, T. and Tanner, T. (1993) Absence of seasonal variation in malaria parasitaemia in an area of intense seasonal transmission. Acta Tropica 54, 5557.CrossRefGoogle Scholar
Snounou, G., Pinheiro, L., Goncalves, L., Fonseca, L., Dias, F., Brown, K. N. and doRosario, V. E. (1993) The importance of sensitive detection of malaria parasites in the human and mosquito hosts in epidemiological studies, as shown by the analysis of field samples from Guinea Bissau. Trans. R. Soc Trop. Med. Hyg. 87, 649653.CrossRefGoogle ScholarPubMed
Tassanakajon, A., Boonsaeng, V., Wilairat, P. and Panyim, S. (1993) Polymerase chain reaction detection of Plasmodium falcipamm in mosquitoes. Trans. R. Soc. Trop. Med. Hyg. 87, 273275.CrossRefGoogle ScholarPubMed
Tirasophon, W., Tassanakajon, A., Boonsaeng, V., Panyim, S. and Wilairat, P. (1993) Sensitive detection of Plasmodium falcipamm in blood and mosquito by DNA amplification. Trans. R. Soc. Trop. Med. Hyg. 35, 117120.Google ScholarPubMed
Vaughan, J., Noden, B. H. and Beier, J. C. (1994) Sporogonie development of cultured Plasmodium falciparum in six species of laboratory-reared Anoplieles mosquitoes. Am. J. Trop. Med. Hyg. 51, 233243.CrossRefGoogle Scholar
Zavala, F., Gwadz, R. W., Collins, F. H., Nussenzweig, R. S. and Nussenzweig, V. (1982) Monoclonal antibodies to circumsporozoite proteins identify the species of malaria parasite in infected mosquitoes. Nature 299, 737738.CrossRefGoogle ScholarPubMed
Zimmerman, P. A., Dadzie, R. Y., De Sole, G., Rema, J., Soumbey, E. and Unnasch, T. R. (1992) Onchocerca volvulus DNA probes classification correlates with epidemiologica! patterns of blindness. J. Infect. Diseases 165, 964968.CrossRefGoogle Scholar